<i>TMC1</i> but Not <i>TMC2</i> Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families-Reference-Cited by-同舟云学术

TMC1 but Not TMC2 Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families

Published:2008 Issue:4 Volume:13 Page:213-218
ISSN:1421-9700
Container-title:Audiology and Neurotology
language:en
Short-container-title:Audiol Neurotol

Author:

Tlili Abdelaziz,Rebeh Imen Ben,Aifa-Hmani Mounira,Dhouib Houria,Moalla Jihen,Tlili-Chouchène Jihen,Said Mariem Ben,Lahmar Imed,Benzina Zeineb,Charfedine Ilhem,Driss Nabil,Ghorbel Abdelmonem,Ayadi Hammadi,Masmoudi Saber

Publisher

S. Karger AG

Subject

Speech and Hearing,Sensory Systems,Otorhinolaryngology,Physiology

Reference17 articles.

1. Inner Ear Pathology in the Deafness Mutant Mouse

2. RNA surveillance: unforeseen consequences for gene expression, inherited genetic disorders and cancer

3. Gorlin RJ: Genetic hearing loss with no associated abnormalities; in Gorlin RJ, Toriello HV, Cohen MM (eds):Hereditary Hearing Loss and Its Syndromes. Oxford, Oxford University Press, 1995, pp 43-61.

4. A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus

5. Four novelTMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss

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